Carbohydrates which differ in configurartion at the glycosidic carbon(i.e.,`C_(1)` in aldose and `C_(2)` in ketoses) are called:

Carbohydrates which differ in configuration at the glycosidic carbon (i.e. C_(1) in aldose and C_(2) in ketoses) are called

Disaccharides linked through the glycosidic carbon atoms of C-(1) of glucose and C_(2) of fructose are ______.

Monosaccharides containing an aldehyde group are called aldoses while those containing aketo group are called ketoses. The aldehyde group is always present at C_1 while the keto group is usually present at C_2 . All monosaccharides containing five and six carbon atoms have cyclic structures, furnaose (five membered) and pyranose (six membered). During ring formation, C_1 in aldoses and C_2 in ketoses becomes chiral and hence all these monosaccharides exist in two stereoisomeric forms called the alpha -anomer and the beta -anomer while C_1 and C_2 are called glycosidic or anomeric carbon atoms. In contrast, stereoisomers, which differ in configuration at any other chiral carbon other than the glycosidic carbon are called epimers. Two molecules of the same or different monosaccharides combine together through glycosidic linkage to form disaccharides. All monosaccharides (aldoses and ketoses) and most disaccharides reduce Tollens'reagent and Fehling's solution, undergo mutarotation and form osazones. Two forms of D-glucopyranose are called

Monosaccharides containing an aldehyde group are called aldoses while those containing aketo group are called ketoses. The aldehyde group is always present at C_1 while the keto group is usually present at C_2 . All monosaccharides containing five and six carbon atoms have cyclic structures, furnaose (five membered) and pyranose (six membered). During ring formation, C_1 in aldoses and C_2 in ketoses becomes chiral and hence all these monosaccharides exist in two stereoisomeric forms called the alpha -anomer and the beta -anomer while C_1 and C_2 are called glycosidic or anomeric carbon atoms. In contrast, stereoisomers, which differ in configuration at any other chiral carbon other than the glycosidic carbon are called epimers. Two molecules of the same or different monosaccharides combine together through glycosidic linkage to form disaccharides. All monosaccharides (aldoses and ketoses) and most disaccharides reduce Tollens'reagent and Fehling's solution, undergo mutarotation and form osazones. Which of the following pairs give the same osazone?

Monosaccharides containing an aldehyde group are called aldoses while those containing aketo group are called ketoses. The aldehyde group is always present at C_1 while the keto group is usually present at C_2 . All monosaccharides containing five and six carbon atoms have cyclic structures, furnaose (five membered) and pyranose (six membered). During ring formation, C_1 in aldoses and C_2 in ketoses becomes chiral and hence all these monosaccharides exist in two stereoisomeric forms called the alpha -anomer and the beta -anomer while C_1 and C_2 are called glycosidic or anomeric carbon atoms. In contrast, stereoisomers, which differ in configuration at any other chiral carbon other than the glycosidic carbon are called epimers. Two molecules of the same or different monosaccharides combine together through glycosidic linkage to form disaccharides. All monosaccharides (aldoses and ketoses) and most disaccharides reduce Tollens'reagent and Fehling's solution, undergo mutarotation and form osazones. Which of the following pairs give positive Tollens' test?